Canonical Allele Identifier: CA2982738
Gene: FGF5 HGNC NCBI

Linked Data

dbSNP Id: rs762447981
gnomAD v2: 4-81207728-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286574A>G , CM000666.2:g.80286574A>G GRCh38
NC_000004.11:g.81207728A>G , CM000666.1:g.81207728A>G GRCh37
NC_000004.10:g.81426752A>G NCBI36
NG_029501.1:g.24987A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.709A>G MANE Select ENSP00000311697.7:p.Lys237Glu
ENST00000312465.11:c.709A>G ENSP00000311697.7:p.Lys237Glu
ENST00000456523.3:c.*233A>G ENSP00000398353.3:n.*233A>G
ENST00000503413.1:n.658A>G
ENST00000507780.1:c.342+11562A>G ENSP00000423903.1:n.342+11562A>G
NM_001291812.1:c.280A>G NP_001278741.1:p.Lys94Glu
NM_004464.3:c.709A>G NP_004455.2:p.Lys237Glu
NM_033143.2:c.*233A>G NP_149134.1:n.*233A>G
NM_001291812.2:c.280A>G NP_001278741.1:p.Lys94Glu
NM_004464.4:c.709A>G MANE Select NP_004455.2:p.Lys237Glu